US4360605A - Mixing component for dental glass ionomer cements - Google Patents
Mixing component for dental glass ionomer cements Download PDFInfo
- Publication number
- US4360605A US4360605A US06/175,389 US17538980A US4360605A US 4360605 A US4360605 A US 4360605A US 17538980 A US17538980 A US 17538980A US 4360605 A US4360605 A US 4360605A
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- United States
- Prior art keywords
- acrylic acid
- copolymer
- maleic acid
- mole
- glass ionomer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/80—Preparations for artificial teeth, for filling teeth or for capping teeth
- A61K6/884—Preparations for artificial teeth, for filling teeth or for capping teeth comprising natural or synthetic resins
- A61K6/887—Compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- A61K6/889—Polycarboxylate cements; Glass ionomer cements
Definitions
- cements which are formed from an inorganic powdery component and an organic polymer comprising carboxylic acid groups have achieved increased importance as filling materials for teeth as well as for fixing materials.
- Carboxylate cements formed from zinc oxide and an aqueous polyacrylic acid solution are known, for example, from German Auslegeschrift No. 16 17 688. Although they are physiologically compatible, they are not suitable as permanent filling materials for aesthetic reasons where they are visible. Further, they show only moderate mechanical strength. Advantageous, however, is that they are chemically bound to the tooth enamel and to dentin. Thus carboxylate cements are broadly used as linings in a tooth cavity and as fixing cements.
- silicate cements which are formed from a silicate glass powder and an aqueous solution of phosphoric acid.
- silicate cements are harmful to the dental pulp and are relatively soluble under oral conditions.
- the former weakness is particularly serious; it necessitates the application of cavity lining agents, procedures which are time consuming and in many cases unreliable.
- Still further cement systems having a powder component consisting of a metal oxide powder, such as zinc oxide, or a silicate cement powder are known from German Auslegeschrift No. 24 39 882.
- a mixing liquid for these cements there are used aqueous solutions of acrylic acid-itaconic acid-copolymers in which the preferred ratio of acrylic acid units to itaconic acid units is in the range of 91:1 to 2:1.
- British Pat. No. 1,382,881 describes glass ionomer cement systems having a mixing component consisting of an aqueous solution of copolymers of unsaturated ⁇ , ⁇ -dicarbocylic acids, which contain more than 50 mole % of unsaturated ⁇ , ⁇ -dicarbocylic acid units.
- maleic acid-itaconic acid-copolymers and copolymers of maleic acid and acrylic or methacrylic acid, comprising more than 90% of maleic acid units are stated.
- the invention relates to dental glass ionomer cements. More particularly, this invention relates to a mixing component for glass ionomer cements, by which a cement is obtained which not only has a good mechanical strength and favourable setting characteristics, but is satisfying in aesthetic and cosmetic respect and has such a good physiological behaviour that it may be used for filling a cavity in a tooth without using a cavity lining agent or similar precautions and, furthermore, has an excellent adhesion to the tooth enamel and to dentin.
- the object of this invention is achieved by using in the preparation of glass ionomer cements a maleic acid-acrylic acid-copolymer having a specifically selected composition.
- a mixing component for glass ionomer cements which may be a liquid mixing component (case a) and in such case consists of an aqueous solution comprising 20 to 65% by weight of a maleic acid-acrylic acid-copolymer and optionally further contains usual additives or may be a solid mixing component (case b) and, in such case, consists of a powder mixture of a glass ionomer cement and a maleic acid-acrylic acid-copolymer, optionally with usual additives.
- the invention is characterized in that the copolymer consists of 20 to 65 mole % acrylic acid units and 80 to 35 mole % maleic acid units.
- acrylic acid-maleic acid-copolymers having the above defined range of composition show especially improved adhesive strength to the dentin and enamel.
- polymaleic acid as a mixing component for glass ionomer cements there is obtained a cement which shows unsatisfactory adhesive strength to the dentin and enamel.
- FIGURE of the accompanying drawing diagrammatically shows the favourable effect achieved by the mixing component according to the invention.
- the curve illustrates the degree of adhesion achieved in relation to the composition of the copolymer.
- copolymers which contain about 40 to 60 mole % acrylic acid units and about 60 to about 40 mole % maleic acid units.
- the molar ratio in any case, is to be understood as the average of all individual molecules of the copolymer.
- the mixing components according to the invention show a remarkably improved compressive strength which may be shown by a comparative example described later.
- the average molecular weight of copolymers useful for the invention may be characterized by their viscosity in aqueous solutions. If the polymer concentration of an aqueous solution is 43%, the viscosity of the aqueous solution is in the range of 0.5 to 1000 Poises, preferably 1 to 100 Poises and more preferably 3 to 50 Poises (each value measured at 25° C.).
- Copolymers having the shown composition may be used for the invention after a usual purification step.
- binary copolymers consisting of acrylic acid and maleic acid units may be used, the copolymers however may also contain minor amounts of additional comonomer units provided that these do not change the characteristics of the copolymer and further provided that the above-defined molar ratio of 20 to 65 molar amounts acrylic acid units to 80 to 35 molar amounts maleic acid units is maintained.
- the powder component of the cement system according to the invention may be a conventional silicate cement powder such as described in German Offenlegungsschrift No. 21 01 889.
- the mixing component of the invention is specifically favourable in combination with calcium aluminum fluorosilicate glass powders which are described in German Offenlegungsschrift No. 20 61 513.
- Useful silicate cement powders further are stated in "Chemical Society Reviews", 7 (2), p. 265 to 296 (1978).
- dental cements are used in the form of a two component system consisting of a liqudid component and a solid powder component.
- the mixing component according to the invention according to one embodiment (a) may be part of the mixing liquid, while according to another embodiment (b) it may be part of the powder component.
- the mixing liquid consists of an aqueous solution of the above defined maleic acid-acrylic acid-copolymer, optionally together with conventional additives.
- the aqueous solution generally contains the copolymer in a concentration of at least 20% by weight, preferably 3 to 60% by weight and more preferably 40 to 50% by weight.
- concentrations are useful for the use as a fixing cement and for prosthetic purposes.
- the copolymer solutions should have a viscosity of at least 0.5 poise, however, not more than 300 Poises.
- the preferred range of viscosity is between 2 and 200, particularly between 5 and 100 poise at 25° C.
- the mixing component i.e., the maleic acid-acrylic acid-copolymer forms part of the powder mixture and is present as a pre-mix consisting of silicate cement powder and maleic acid-acrylic acid-copolymer in solid form.
- the powder component then may be mixed with water, optionally together with conventional additives.
- additives such as chelating agents, preferably tartaric acid
- tartaric acid may be incorporated into the powder component and/or into the liquid component in order to improve the setting characteristic (German Offenlegungsschrift No. 23 19 715).
- the addition of tartaric acid has no influence on the adhesion of the resulting cement to the tooth enamel and dentin.
- a cow's tooth is faced and the enamel layer is polished and kept free of fat.
- the tooth is embedded in plaster and the treated surface is adjusted in a plane parallel to the measuring table.
- the calcium aluminum-fluoro-silicate glass powder is pasted with the approximately 44% aqueous solution of the respective copolymer in a weight ratio of about 3.0:1.
- a steel cylinder of a length of 30 mm. and diameter of 8 mm. is filled with this cement composition. At a distance of 3 mm. from the inlet opening a wire of 1 mm. diameter is inserted by bores in order to provide a more suitable retention of the filling cement within the cylinder.
- the steel cylinder is placed on the plane tooth surface and loaded for 10 min. with a mass of 100 g.
- the teeth carrying the bodies that are to be drawn off are stored in the following manner:
- the steel cylinder After storing, the steel cylinder is drawn off with an advance of 4 mm. per minute on a suitable testing machine. The force required for drawing off the steel cylinder is recorded and shows upon multiplication with the factor 3.5 the adhesion in kiloponds per cm 2 . The said measuring is effected with the same cement composition on 5 different teeth and the average is calculated therefrom.
- the measuring of the viscosity of the copolymer solution was effected with the aid of a rotational viscosimeter.
- a rotational viscosimeter For this purpose an apparatus, identified by the name HAAKE ROTO VISKO, with a rotating body HV I, gear number 3, engine speed number 1 and calibration constant 48.5 was used.
- the absolute viscosity in Centiposes is obtained by multiplication of the scale reading with said three parameters.
- An acrylic acid-maleic acid-copolymer (molar ratio 3:2), suitable for dental medical purposes is mixed with water to a concentration of about 43% by weight.
- the solution has a viscosity of 12 poise/25° C.
- This liquid is mixed with a commercial silicate cement powder (Syntrex) in a weight ratio of 1:2.5, to obtain a paste that is well suitable for clinical purposes.
- the paste is introduced in known manner into prepared tooth cavities.
- the mixture hardens after a few minutes and has in the set state a transparency corresponding to the natural tooth.
- the filling shows good adhesion to the cleaned tooth substance, even if the usual mechanical retentions are not prepared.
- a copolymer having a molar ratio of maleic acid:acrylic acid of 1:1 is used according to example 1 to prepare a mixing liquid for dental cements.
- a commercial glass ionomer cement powder (G.C.'s Fuji) is mixed with this liquid in a weight ratio of 2.3:1 to form a paste.
- the thus obtained cement is useful as a filling material for tooth cavities.
- the adhesive strength to the tooth enamel amounts to 50 kp per cm 2 .
- the compressive strength is 1.860 kp/cm 2 .
- the copolymer of example 2 is dissolved in water to form an aqueous solution of a concentration of 35% by weight (viscosity: 3 poise/25° C.). After this liquid has been mixed with commercial glass ionomer cement powder for fixing use (De Trey Chem-Bond), in a powder-liquid-ratio of 1.2:1, a thin-flowing cement is obtained which shows good adhesion to the tooth substance and has a compressive strength of 1.100 kp per cm 2 .
- 240 mg-portions of a commercial glass ionomer cement powder are filled into the mixing compartment of shaking caps according to German Offenlegungsschrift No. 19 10 885.
- this capsule contains a foil bag from plastic covered aluminum, which is filled with 96 mg of the copolymer solution described in example 1.
- a filled capsule is used, as described in DE-OS No. 19 10 885, after mixing by means of a mechanical mixing device a cement is obtained which is useful as a permanent filling material for tooth cavities (specifically for cervical lesions) and which has a good adhesive strength to the tooth substance.
- a dry intimate mixture from 300 mg commercially available glass ionomer cement powder (ASPA) and 41 mg of the copolymer mentioned in example 2 is compressed in the usual manner to form a tablet. After short wetting of this tablet in 59 mg of a 14% tartaric acid solution the tablet may easily be mixed to form a cement paste which is well suited for filling cervical lesions and shows good adhesive strength to the tooth substance.
- ASPA commercially available glass ionomer cement powder
- 41 mg of the copolymer mentioned in example 2 is compressed in the usual manner to form a tablet. After short wetting of this tablet in 59 mg of a 14% tartaric acid solution the tablet may easily be mixed to form a cement paste which is well suited for filling cervical lesions and shows good adhesive strength to the tooth substance.
- This example shows that according to the invention the compressive strength is improved over a known polycarboxylate cement based on acrylic acid-itaconic acid-copolymers.
- the compressive strength of the cement prepared by using a mixing liquid according to the invention is about 25% higher than that obtained with the known mixing liquid.
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- Health & Medical Sciences (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Plastic & Reconstructive Surgery (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Dental Preparations (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Description
______________________________________ RESULTS Compressive Mixing Liquid Strength ______________________________________ Acrylic acid-itaconic acid-copolymer 1320 kp/cm.sup.2 (De Trey, ASPA liquid) According to the invention, acrylic 1680 kp/cm.sup.2 acid-maleic acid-copolymer (molar ratio 1:1) ______________________________________
Claims (10)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2932823 | 1979-08-13 | ||
DE19792932823 DE2932823A1 (en) | 1979-08-13 | 1979-08-13 | MIXING COMPONENT FOR GLASIONOMER CEMENTS |
Publications (1)
Publication Number | Publication Date |
---|---|
US4360605A true US4360605A (en) | 1982-11-23 |
Family
ID=6078393
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US06/175,389 Expired - Lifetime US4360605A (en) | 1979-08-13 | 1980-08-05 | Mixing component for dental glass ionomer cements |
Country Status (7)
Country | Link |
---|---|
US (1) | US4360605A (en) |
EP (1) | EP0024056B1 (en) |
JP (1) | JPS5692804A (en) |
AT (1) | ATE16683T1 (en) |
AU (1) | AU531850B2 (en) |
CA (1) | CA1154891A (en) |
DE (2) | DE2932823A1 (en) |
Cited By (91)
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US4482535A (en) * | 1980-10-03 | 1984-11-13 | Andras Sugar | Cosmetic preparation for teeth |
WO1988001859A1 (en) * | 1986-09-15 | 1988-03-24 | Den Mat Corporation | Dental compositions incorporating glass ionomers |
US4808228A (en) * | 1987-02-20 | 1989-02-28 | Minnesota Mining And Manufacturing Company | Glass ionomer cement powder |
US4861808A (en) * | 1986-04-08 | 1989-08-29 | Dentsply Limited | Glass/poly (carboxylic acid) cement compositions |
USRE33100E (en) * | 1986-09-15 | 1989-10-24 | Den-Mat Corporation | Dental compositions incorporating glass ionomers |
DE4019617A1 (en) * | 1990-06-20 | 1992-01-02 | Thera Ges Fuer Patente | IMPLANTABLE ACTIVE SUBSTITUTE MATERIAL |
US5130347A (en) * | 1987-12-30 | 1992-07-14 | Minnesota Mining And Manufacturing Company | Photocurable ionomer cement systems |
US5147904A (en) * | 1989-08-24 | 1992-09-15 | Thera Patent Gmbh & Co. Kg | Open-pored moldings, a process for their production and use thereof |
US5156835A (en) * | 1987-01-30 | 1992-10-20 | Colgate-Palmolive Company | Antibacterial antiplaque oral composition |
US5178851A (en) * | 1987-01-30 | 1993-01-12 | Colgate-Palmolive Company | Antiplaque antibacterial oral composition |
US5180578A (en) * | 1987-01-30 | 1993-01-19 | Colgate-Palmolive Company | Antibacterial antiplaque anticalculus oral composition |
US5188821A (en) * | 1987-01-30 | 1993-02-23 | Colgate-Palmolive Company | Antibacterial antiplaque oral composition mouthwash or liquid dentifrice |
US5192531A (en) * | 1988-12-29 | 1993-03-09 | Colgate-Palmolive Company | Antibacterial antiplaque oral composition |
US5192530A (en) * | 1987-01-30 | 1993-03-09 | Colgate-Palmolive Company | Antibacterial antiplaque oral composition |
US5227413A (en) * | 1992-02-27 | 1993-07-13 | Minnesota Mining And Manufacturing Company | Cements from β-dicarbonyl polymers |
US5314474A (en) * | 1989-03-09 | 1994-05-24 | Thera Patent Gmbh & Co. Kg, Gesellschaft Fur Industrielle Schutzrechte | Bone replacement part made of glass ionomer cement |
US5318929A (en) * | 1990-02-12 | 1994-06-07 | Thera Patent Gmbh & Co. Kg Gesellschaft Fur Industrielle Schutzrechte | Apatite glass ceramic |
US5369142A (en) * | 1993-01-15 | 1994-11-29 | The Ohio State University | Water soluble polymers containing amino acid residues for dental restoratives |
US5814682A (en) * | 1996-06-14 | 1998-09-29 | Rusin; Richard P. | Method of luting a provisional prosthetic device using a glass ionomer cement system and kit therefor |
US5922786A (en) * | 1997-04-11 | 1999-07-13 | Minnesota Mining And Manufacturing Company | Dental primer composition |
US5955514A (en) * | 1993-04-19 | 1999-09-21 | Dentsply Research & Development Corp. | Dental composition and method |
US6136885A (en) * | 1996-06-14 | 2000-10-24 | 3M Innovative Proprerties Company | Glass ionomer cement |
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DE3248357A1 (en) * | 1982-12-28 | 1984-07-05 | ESPE Fabrik pharmazeutischer Präparate GmbH, 8031 Seefeld | POWDER-SHAPED DENTAL MATERIAL, METHOD FOR THE PRODUCTION THEREOF AND ITS USE |
JPS6081115A (en) * | 1983-10-11 | 1985-05-09 | Tokuyama Soda Co Ltd | dental cement |
JPS61229806A (en) * | 1985-04-05 | 1986-10-14 | G C Dental Ind Corp | Dental aluminic acid cement composition |
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Also Published As
Publication number | Publication date |
---|---|
ATE16683T1 (en) | 1985-12-15 |
CA1154891A (en) | 1983-10-04 |
EP0024056A2 (en) | 1981-02-18 |
EP0024056B1 (en) | 1985-11-27 |
JPH0262525B2 (en) | 1990-12-26 |
AU531850B2 (en) | 1983-09-08 |
DE2932823A1 (en) | 1981-03-12 |
AU6140780A (en) | 1981-02-19 |
DE3071262D1 (en) | 1986-01-09 |
JPS5692804A (en) | 1981-07-27 |
EP0024056A3 (en) | 1982-05-05 |
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